Sabina Liechti‐Gallati

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

Anthony P. Monaco, Corlee J. Bertelson, Sabina Liechti‐Gallati et al. · Genomics · 1988 · 1.2K citations

Life Sciences, Genetics, Molecular Genetics +11

Protease-Antiprotease Imbalance in the Lungs of Children with Cystic Fibrosis

P. Birrer, Noel G. McElvaney, A Rüdeberg et al. · American Journal of Respiratory and Critical Care Medicine · 1994 · 381 citations

Veterinary Medicine, Immunology, Pediatrics +16

Association of two silent polymorphisms of platelet glycoprotein la/lla receptor with risk of myocardial infarction: a case-control study

Khatereh Moshfegh, Walter A. Wuillemin, Maurice Redondo et al. · The Lancet · 1999 · 188 citations

Medicine, Genetics, Molecular Genetics +13

Clonality and X-inactivation patterns in hematopoietic cell populations detected by the highly informative M27 beta DNA probe [see comments]

MF Fey, Sabina Liechti‐Gallati, A. von Rohr et al. · Blood · 1994 · 136 citations · Full text

Life Sciences, Genetics, Hematology +14

On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.

T. Grimm, Sabina Liechti‐Gallati, T. Bettecken et al. · Journal of Medical Genetics · 1994 · 108 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17